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AAMI ANSI/AAMI/ISO 17664-1:2022

Processing of health care products—Information to be provided by the medical device manufacturer for the processing of medical devices—Part 1: Critical and semi-critical medical devices
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AAMI ANSI/AAMI/ISO 17664-1:2022

Processing of health care products—Information to be provided by the medical device manufacturer for the processing of medical devices—Part 1: Critical and semi-critical medical devices

PUBLISH DATE 2022
AAMI ANSI/AAMI/ISO 17664-1:2022
Specifies requirements for the information to be provided by the medical device manufacturer for the processing of a medical device that requires sterilization or disinfection to ensure that the device is safe and effective for its intended use. This includes information for processing prior to use or reuse of the medical device. Applicable for medical devices that are intended for invasive or other direct patient contact or that otherwise present the risk of transmission of infectious agents. Specifies requirements to assist manufacturers of medical devices in providing detailed instructions for processing that consists of the following activities where applicable: pre-treatment at the point of use; preparation, cleaning, disinfection; drying; inspection, maintenance and testing; packaging; sterilization; storage; transportation. Supersedes: ANSI/AAMI/ISO 17664:2017
SDO AAMI: Assoc. for the Advancement of Medical Instrumentation
Document Number 17664-1
Publication Date Dec. 21, 2022
Language en - English
Page Count 38
Revision Level
Supercedes
Committee
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